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1-Methoxy-2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane is a complex organic compound with the molecular formula C6H15NO3Si. It is a cyclic structure containing a silicon atom, three oxygen atoms, and a nitrogen atom, with a methoxy group attached to the silicon. 1-Methoxy-2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecane is known for its unique properties, such as its ability to act as a ligand in coordination chemistry, particularly in the formation of metal complexes. It is also of interest in the field of organosilicon chemistry due to its potential applications in material science and as a precursor in the synthesis of more complex silicon-containing molecules. The compound's structure and reactivity make it a subject of study for researchers exploring the boundaries of silicon-based chemistry and its implications in various industrial and academic settings.

4025-80-3

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4025-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4025-80-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4025-80:
(6*4)+(5*0)+(4*2)+(3*5)+(2*8)+(1*0)=63
63 % 10 = 3
So 4025-80-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO4Si/c1-9-13-10-5-2-8(3-6-11-13)4-7-12-13/h2-7H2,1H3

4025-80-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecane

1.2 Other means of identification

Product number -
Other names 5-methoxy-silitrane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4025-80-3 SDS

4025-80-3Downstream Products

4025-80-3Relevant academic research and scientific papers

A new route to silicon alkoxides from silica

Kemmitt, Tim,Henderson, William

, p. 1031 - 1035 (2007/10/03)

A novel route to tetraethoxysilane and other silicon alkoxides is described, from amorphous silica (SiO2·H2O) as the raw material. The reaction of amorphous silica with triethanolamine is enhanced by using an alkali metal hydroxide catalyst, to form a range of triethanolamine-substituted silatrane species. These can undergo alkoxide exchange in acidic alcohols to form alkoxysilatranes, tetraalkoxysilanes, hexaalkoxydisiloxanes and higher siloxanes. Reaction of triethanolamine-substituted silatranes with acetic anhydride produces acetoxysilatrane. Products were identified by multinuclear (1H, 13C and 29Si) magnetic resonance spectroscopy, electrospray mass spectrometry or high-resolution gas chromatography electron impact mass spectrometry.

1-Halosilatranes

Voronkov, M. G.,Baryshok, V. P.,Petukhov, L. P.,Rakhlin, V. I.,Mirskov, R. G.,Pestunovich, V. A.

, p. 39 - 56 (2007/10/02)

The electronic structure of 1-halosilatranes is discussed.Some new preparative methods based on hetero- and homo-lytic reactions of the silatrane and the Si- and C-substituted silatranes with halogenating reagents are described and also synthetic routes to 1-halosilatranes from certain organotrialkoxy- and organotrichlorosilanes.The electrophilic reactions of 1-iodosilatrane with ethers and esters, carbonyl compounds, alkoxysilanes and siloxanes, terminal alkynes and organomercurials have been studied

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